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Aerobic alcohol oxidation catalyzed by supported ruthenium hydroxides

机译:负载的氢氧化钌催化好氧醇氧化

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The supported ruthenium hydroxide (Ru(OH)_x) catalysts prepared with three different TiO_2 supports and an Al_2O_3 support showed the high catalytic activity for the oxidation of alcohols with molecular oxygen. In the presence of the most active catalyst, various kinds of alcohols could be converted into the corresponding carbonyl compounds in high yields. In addition, the catalyst could be applied to the aerobic amine oxidation. The observed catalysis was truly heterogeneous and the catalyst retrieved after the reaction could be reused with keeping its high catalytic performance. A reaction mechanism involving the ruthenium alcoholate formation/hydride abstraction (β-elimination) has been proposed. The alcoholate formation and hydride abstraction are reversible reactions. The kinetic isotope effects (k_H/k_D = 4.9–5.3) show that the C–H bond breaking is included in the rate-determining step. The present Ru(OH)_x-catalyzed aerobic alcohol oxidation was dependent on the coordination number (CN) of nearest-neighbor Ru atoms in Ru(OH)_x and the suitable CN existed.
机译:用三种不同的TiO_2载体和Al_2O_3载体制备的负载型氢氧化钌(Ru(OH)_x)催化剂对醇与分子氧的氧化具有很高的催化活性。在活性最高的催化剂的存在下,各种醇都可以高产率转化为相应的羰基化合物。另外,该催化剂可用于需氧胺的氧化。观察到的催化是真正的多相反应,反应后回收的催化剂可以在保持其高催化性能的情况下重复使用。已经提出了涉及钌醇盐形成/氢化物提取(β-消除)的反应机理。醇化物的形成和氢化物的提取是可逆的反应。动力学同位素效应(k_H / k_D = 4.9–5.3)表明,速率决定步骤中包括C–H键断裂。目前Ru(OH)_x催化的好氧醇氧化取决于Ru(OH)_x中最近邻Ru原子的配位数(CN),并且存在合适的CN。

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